반응 #880
ord-7962a8e3cbfa49e3aabf54e37edc9672
반응 방정식
반응 조건
후처리
- 1기타reacted at room temperature for 3 hrs
- 2workup.ADDITIONwas slowly added to the reaction mixture
- 3기타subjected to reaction at room temperature for 4 hrs
- 4기타After completion of the reaction
- 5여과the produced solid by-product was filtered off
- 6세척washed with distilled water and saturated saline
- 7세척The organic phase washed
- 8건조was dried over anhydrous magnesium sulfate
- 9기타the solvent was removed by distillation under reduced pressure
- 10기타The reaction mixture was purified by Silica gel column chromatography
실험 절차
In another 2 liter flask, 57.2 g of methyl triphenylphosphonium bromide was placed. 500 ml of anhydrous ether was poured and then, stirred. To the resulting solution was slowly added 18.0 g of potassium tert-butoxide and reacted at room temperature for 3 hrs. 25.6 g of the above 4-(2-[1,3]-dioxane-2-yl-ethoxy)benzaldehyde was dissolved in 200 ml of anhydrous ether and was slowly added to the reaction mixture and then subjected to reaction at room temperature for 4 hrs. After completion of the reaction, the produced solid by-product was filtered off and washed with distilled water and saturated saline. The organic phase washed was dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure. The reaction mixture was purified by Silica gel column chromatography to obtain 19.7 g of 2-[2-(4-vinylphenoxy)ethyl]-[1,3]-dioxane, represented by the following formula: ##STR9##